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Published ahead of print on September 15, 2006, doi:10.1165/rcmb.2006-0331TR
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American Journal of Respiratory Cell and Molecular Biology. Vol. 36, pp. 158-165, 2007
© 2007 American Thoracic Society
DOI: 10.1165/rcmb.2006-0331TR


HEME OXYGENASE-1: A MULTIFACETED TRIPLE-THREAT MOLECULE

The Role of Heme Oxygenase-1 in Pulmonary Disease

Laura E. Fredenburgh, Mark A. Perrella and S. Alex Mitsialis

Division of Pulmonary and Critical Care Medicine, Department of Medicine, Brigham and Women's Hospital; and Division of Newborn Medicine, Children's Hospital, Boston, Massachusetts

Correspondence and requests for reprints should be addressed to Laura E. Fredenburgh, Division of Pulmonary and Critical Care Medicine, Brigham and Women's Hospital, 75 Francis Street, Boston, MA 02115. E-mail: lfredenburgh{at}partners.org

Abstract

Heme oxygenase (HO)-1, the inducible isoform of heme oxygenase, is a cytoprotective enzyme that plays a central role in the defense against oxidative and inflammatory insults in the lung. HO-1 catalyzes the degradation of heme, a potent oxidant, into biliverdin, iron, and carbon monoxide (CO). These downstream products of heme catabolism have recently been found to mediate the antioxidant, antiapoptotic, antiproliferative, vasodilatory, and anti-inflammatory properties of HO-1. Although absence of HO-1 is rare in humans, a number of HO-1 promoter polymorphisms have been identified that may influence HO-1 expression in vivo and lead to disease states. This review will summarize studies that implicate HO-1 and heme metabolites in the pathophysiology of pulmonary disease and discuss recent advances in the therapeutic applications of HO-1.

Key Words: HO-1 • polymorphism • ARDS • pulmonary hypertension • COPD


CLINICAL RELEVANCE

HO-1 plays a key role in the defense against oxidative and inflammatory insults in the lung. This review summarizes studies that implicate HO-1 in pulmonary disease and recent advances in the therapeutic applications of HO-1.

 



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